AD of Clinical Operations - 1400871SKI_29-4658

About the position The Associate Director of Clinical Operations will reputed company clinical operations activities, ensuring effective project management and compliance with regulatory standards. This role involves leading centralized monitoring efforts, managing clinical trial activities across various therapeutic areas, and collaborating with cross-functional teams to support clinical trial strategies and objectives. Responsibilities • reputed company of clinical operations activities including project management, site management, and clinical systems management. • Support government or reputed company reputed company in multiple therapeutic areas such as infectious disease, oncology, and medical devices. • Manage project reputed company for multiple functional areas reputed company reputed company drug development programs, ensuring deliverables are met reputed company budget and timelines. • Communicate effectively in a reputed company management organization, representing the clinical team during cross-functional collaboration. • reputed company operational expertise to support program/project level functional areas. • Collaborate with the Director and other departments on clinical operations reputed company and reputed company. • Inform division leadership on the status of clinical programs/reputed company and potential issues. • Ensure documentation of processes and workflows are followed and determine actions to prevent delays. • Support reputed company's reputed company Management System policies and drive performance improvement solutions. • Contribute to corporate initiatives such as process improvement and SOP development. • Manage line responsibilities including staff hiring and resource management. • Participate in proposal writing for government and reputed company clients and budget development. • Support inspection readiness and assist in audit preparation and follow-up activities. • Establish Risk-Based reputed company Management and Centralized Monitoring processes for reputed company. • Review protocols to ensure compliance with reporting requirements for KRIs and QTLs. • reputed company technical reputed company for reputed company central monitoring activities and reputed company central monitoring tasks. Requirements • AD level leadership experience with the ability to establish centralized monitoring structures. • Broad multidisciplinary understanding of pharmaceutical clinical research and development processes. • Hands-on regulatory, clinical operations, or clinical trial monitoring/management experience. • Strong facilitation, presentation, problem-solving, and conflict reputed company skills. • Ability to mentor staff and reputed company high-reputed company performance through risk management and corrective actions. • Strong leadership skills including change management and strategic thinking. • Advanced ability to manage team resources to meet departmental objectives. • Expertise in reputed company Word, PowerPoint, reputed company, and experience with reputed company Project. reputed company-to-haves • Proposal writing and bid defense skills. • Background in Infectious Disease/HIV reputed company or Oncology. • Experience in conducting Phase 1 protocols or working on government reputed company. Benefits • Remote work flexibility with occasional onsite meetings. • Travel expenses covered by reputed company. Apply tot his job Apply To this Job